脂解
脂肪细胞
脂肪酶
生物
染色质免疫沉淀
内科学
脂肪组织
内分泌学
分解代谢
能量稳态
激素敏感脂肪酶
化学
生物化学
酶
基因表达
新陈代谢
基因
医学
发起人
肥胖
作者
Yang Chen,Lin Liu,Ryan Calhoun,Lan Cheng,David Merrick,David J. Steger,Patrick Seale
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-01-03
卷期号:11 (1)
被引量:1
标识
DOI:10.1126/sciadv.ads5963
摘要
Adipocyte lipolysis controls systemic energy levels and metabolic homeostasis. Lipolysis is regulated by posttranslational modifications of key lipolytic enzymes. However, less is known about the transcriptional mechanisms that regulate lipolysis. Here, we identify interferon regulatory factor–2 binding protein 2 (IRF2BP2) as a transcriptional repressor of adipocyte lipolysis. Deletion of IRF2BP2 in human adipocytes increases lipolysis without affecting glucose uptake, whereas IRF2BP2 overexpression decreases lipolysis. RNA sequencing, and chromatin immunoprecipitation sequencing analyses show that IRF2BP2 represses lipolysis-related genes, including LIPE , which encodes hormone sensitive lipase, the rate-limiting enzyme in lipolysis. Adipocyte-selective deletion of Irf2bp2 in mice increases Lipe expression and free fatty acid levels, resulting in adipose tissue inflammation and glucose intolerance. Together, these findings demonstrate that IRF2BP2 restrains adipocyte lipolysis and opens avenues to target lipolysis for the treatment of metabolic disease.
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